Discover and read the best of Twitter Threads about #GPnews
Most recents (5)
@sepidgar2 Philanthropic endeavours - a great disguise for terrible crimes
As is the #CrimesAgainstHumanity currently committed under the disguise of “sustainability “
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As is the #CrimesAgainstHumanity currently committed under the disguise of “sustainability “
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@sepidgar2 Including funnelling children into abusive social care system via increasing false accusations of factitious induced illness & medically unexplained symptoms ,under the guise of “parity for mental health “ & “sustainability” of private NHS joint providers of health & social care
@sepidgar2 Including negative affects of geo engineering on the natural world & #climate
Seeding oceans, stratospheric aerosols , blocking the sun with dust, to “save the planet from climate change”
As we “save the NHS” through #MUSviolationsHour of the chronically ill & vaccine injured
Seeding oceans, stratospheric aerosols , blocking the sun with dust, to “save the planet from climate change”
As we “save the NHS” through #MUSviolationsHour of the chronically ill & vaccine injured
Review protocols so 'robust' That Cochrane continues to endorse graded exercise therapy as a treatment for ME even though the decision is based on extremely poor quality research and flies in the face of the experience of millions ME sufferers. #pwME #MyalgicE #StopGET #MEcfs
Cochrane’s decision also ignores more and more research like this demonstrating the negative effect exercise has on ME. #pwME #MyalgicE #ScienceNotStigma #MedEd #MEcfs #health #GPnews
healthrising.org/blog/2019/10/1…
healthrising.org/blog/2019/10/1…
Are Cochrane’s editors unduly influenced by the authors of the flawed research? How else can their decision to defend research that's dismissed by academics around the world be explained? How can they ignore the mounting evidence that shows exercise harms people with ME?
Very disappointing indeed to see @SAGEPublishers publishing harmful and demonstrably inaccurate information about the treatment of ME/CFS. 1/ #pwME #MyalgicE #MedEd #MEcfs #health #NHS #GPnews #Research #SAGE
'Mitochondrial alterations in NK lymphocytes from ME/CFS patients' published in The Journal of Immunology. #pwME #MyalgicE #MedEd #MEcfs #health #research
#ScienceNotStigma #GPnews
jimmunol.org/content/202/1_…
#ScienceNotStigma #GPnews
jimmunol.org/content/202/1_…
"ME/CFS patients have impaired natural killer (NK) cell activity. NK lymphocytes are a critical first defense against viruses and cancer. ME/CFS patients have difficulties controlling viral infections and many develop non-Hodgkin’s lymphoma."
"In our study, we observed that the two main energy-generating mitochondrial pathways, oxidative phosphorylation and glycolysis (bioenergetics parameters), are deregulated in ME/CFS NK cells and in peripheral blood mononuclear cells (PBMCs)."
I so wish I had something good to share about GPs but here I am again drawing attention to poor practice. Telling patients with ME they're 'hyper-sensitive' to their symptoms, implying they somehow aren't real, is textbook gaslighting bordering on psychological abuse. 1/ #NHS
